HGVS | Genome Assembly |
---|---|
NC_000009.12:g.6592915A= , CM000671.2:g.6592915A= | GRCh38 |
NC_000009.11:g.6592915A= , CM000671.1:g.6592915A= | GRCh37 |
NC_000009.10:g.6582915A= | NCBI36 |
NG_016397.1:g.57778T= , LRG_643:g.57778T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000321612.8:c.1337T= MANE Select | ENSP00000370737.4:p.Val446= | |
ENST00000639364.1:n.1037T= | ||
ENST00000639443.1:n.905T= | ||
ENST00000639493.1:n.489T= | ||
ENST00000639954.1:n.1045T= | ||
ENST00000640592.1:n.1220T= | ||
ENST00000640703.1:n.180T= | ||
ENST00000321612.6:c.1337T= | ENSP00000370737.3:p.Val446= | |
ENST00000463305.1:n.421T= | ||
NM_000170.2:c.1337T= , LRG_643t1:c.1337T= | NP_000161.2:p.Val446= | |
NM_000170.3:c.1337T= MANE Select | NP_000161.2:p.Val446= |